An 283 Reaktionen beteiligt

5708

Cl
Reaction #3089
HCl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC(CC)CC1(C(=O)Cl)CCCCC1
Reaction #42026
1-(2-ethyl-butyl)-cyclohexanecarbonyl chloride
Ausbeute 96.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCC(CC)CC1(C(=O)Cl)CCCCC1
Reaction #42027
1-(2-ethyl-butyl)-cyclohexanecarbonyl chloride
Ausbeute 92.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCC(CC)CC1(C(=O)Cl)CCCCC1
Reaction #42028
1-(2-ethyl-butyl)-cyclohexanecarbonyl chloride
Ausbeute 92.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCC(CC)CC1(C(=O)Cl)CCCCC1
Reaction #42029
1-(2-ethyl-butyl)-cyclohexanecarbonyl chloride
Ausbeute 95.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(OC1c2ccccc2C(=O)N1c1ccc2ccc(Cl)nc2n1)N1CCN(C(=O)C2CCCCC2)CC1
Reaction #55357
2-(7-Chloro-1,8-naphthyridin-2-yl)-3-(4-cyclohexylcarbonylpiperazin-1-yl)carbonyloxy-isoindolin-1-one
Ausbeute 69.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
O=C(Nc1ccc(-c2ccccc2)s1)C1CCCCC1
Reaction #55944
compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CCC(NC(C)C)C(OC(=O)C1CCCCC1)c1ccc(Oc2ccccc2C)c2[nH]c(=O)ccc12.Cl
Reaction #56062
8-toluyloxy-5-(1-cyclohexylcarbonyloxy-2-isopropylaminobutyl)carbostyril hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
O=C(NCC1(c2ccc(Br)cc2)c2ccccc2-c2nccn21)C1CCCCC1
Reaction #74449
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(CSCCOC(=O)C1CCCCC1)NC/C=C\COc1cc(CN2CCCCC2)ccn1
Reaction #80333
title compound
Ausbeute 35.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@]2(C)[C@H]1OC(=O)COC(=O)C1CCCCC1
Reaction #93007
above-identified compound
Ausbeute 88.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
O=C(NNc1ccc(F)cn1)C1CCCCC1
Reaction #162803
title compound
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(OCCc1ccccc1)C1CCCCC1
Reaction #174901
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN(C(=O)C1CCCCC1)C(CC1CCCCC1)CN1CCN(c2cccc3[nH]ccc23)CC1
Reaction #183752
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(C1CCCCC1)N1CCC(Nc2nc(-c3ccccc3)c3ccccc3n2)CC1
Reaction #184727
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN1CCC(c2c[nH]c3ccc(NC(=O)C4CCCCC4)cc23)CC1
Reaction #187287
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cn1cncc1C(O)(c1ccc(Cl)cc1)c1ccc2nc(NC(=O)C3CCCCC3)nc(-c3cccc(Cl)c3)c2c1
Reaction #194987
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(NC(CC1CCCCC1)CN1CCN(c2nc3ccccc3s2)CC1)C1CCCCC1
Reaction #195172
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(CSCCOC(=O)C1CCCCC1)NCC=CCOc1cc(CN2CCCCC2)ccn1
Reaction #201003
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccccc1N1CCN(CC(CC2CCCCC2)N(C)C(=O)C2CCCCC2)CC1
Reaction #205369
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Seite 1Weiter